细胞生物学
肝细胞
Wnt信号通路
过氧化物酶体增殖物激活受体
核受体
心理压抑
基因敲除
化学
过氧化物酶体增殖物激活受体α
生物
癌症研究
基因表达
信号转导
受体
生物化学
转录因子
基因
体外
作者
Daisuke Aibara,Shogo Takahashi,Tomoki Yagai,Donghwan Kim,Chad Brocker,Moshe Levi,Kimihiko Matsusue,Frank J. Gonzalez
出处
期刊:iScience
[Cell Press]
日期:2022-04-01
卷期号:25 (5): 104196-104196
被引量:6
标识
DOI:10.1016/j.isci.2022.104196
摘要
Peroxisome proliferator-activated receptor α (PPARA) is a key mediator of lipid metabolism and inflammation. Activation of PPARA in rodents causes hepatocyte proliferation, but the underlying mechanism is poorly understood. This study focused on genes repressed by PPARA and analyzed the mechanism by which PPARA promotes hepatocyte proliferation in mice. Activation of PPARA by agonist treatment was autoregulated, and induced expression of the epigenetic regulator UHRF1 via activation of the newly described PPARA target gene E2f8, which, in turn, regulates Uhrf1. UHRF1 strongly repressed the expression of CDH1 via methylation of the Cdh1 promoter marked with H3K9me3. Repression of CDH1 by PPARA activation was reversed by PPARA deficiency or knockdown of E2F8 or UHRF1. Furthermore, a forced expression of CDH1 inhibited expression of the Wnt signaling target genes such as Myc after PPARA activation, and suppressed hepatocyte hyperproliferation. These results demonstrate that the PPARA-E2F8-UHRF1-CDH1 axis causes epigenetic regulation of hepatocyte proliferation.
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